Senior SDTM Programmer & Data Strategy Lead

Bristol Myers Squibb

Denham

On-site

GBP 70,000 - 110,000

Full time

36 hours ago
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Job summary

Bristol Myers Squibb is seeking a Senior SDTM Statistical Programmer to lead SDTM strategies across studies from protocol review to global regulatory submission. You will guide CROs and internal teams, mentoring juniors and ensuring top-quality deliverables that support regulatory approvals.

With deep CDISC/SDTM expertise and advanced SAS skills, you will operate at the intersection of science, data, and regulatory science, driving process improvements and maintaining high standards in a

Qualifications

  • 4+ years of pharmaceutical or CRO experience as a SAS Programmer supporting clinical trials and regulatory submissions.
  • Deep expertise in CDISC/SDTM standards and understanding of the clinical development lifecycle.
  • Exceptional SAS programming skills (Base, Stat, Graph) and experience with multi-source data environments.

Responsibilities

  • Provide technical leadership for assigned studies, shaping SDTM strategies from protocol review through to global regulatory submission.
  • Lead CRO and vendor programming activities and mentor junior programmers.
  • Collaborate with cross-functional study teams to ensure high-quality, timely deliverables for regulatory submissions.
  • Develop leadership presence and drive quality outcomes across projects.

Skills

SAS programming
CDISC/SDTM standards
Data management in clinical trials
Cross-functional collaboration
Problem solving

Education

BA/BS or above in a relevant field

Tools

Base SAS
SAS Graph

Job description

Bristol Myers Squibb is seeking a Senior SDTM Statistical Programmer to lead SDTM strategies across studies from protocol review to global regulatory submission. You will guide CROs and internal teams, mentoring juniors and ensuring top-quality deliverables that support regulatory approvals.

With deep CDISC/SDTM expertise and advanced SAS skills, you will operate at the intersection of science, data, and regulatory science, driving process improvements and maintaining high standards in a

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